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Human leukocyte antigen A2 or A3 (HLA-A2 (for allele *A*02) and HLA-A3 (for allele *A*03))

Target
HLA-A2 (for allele *A*02) and HLA-A3 (for allele *A*03)
Molecular classification
Major histocompatibility complex class I protein, Transmembrane glycoprotein, Antigen-presenting molecule, Receptor
01

Overview

Human leukocyte antigen A2 and A3 are polymorphic cell surface proteins belonging to the major histocompatibility complex class I family. They are encoded by separate alleles at the HLA-A locus, and are responsible for presenting short peptide fragments—derived from endogenous proteins or intracellular pathogens—to cytotoxic T lymphocytes. This interaction is a cornerstone of immune recognition, driving the destruction of infected, mutated, or foreign cells by the host immune system. HLA-A2 and HLA-A3 differ in their peptide-binding motifs and genetic sequence, which impact immune responses and clinical outcomes in transplantation, infection, and cancer. Both are of major focus in immunotherapy and vaccine design, owing to their high prevalence and functional importance in human health and disease.

Other names
HLA-A*02 (or HLA-A2)HLA-A*03 (or HLA-A3)HLA-A supertypesA2 supertypeA3 supertype
02

Mechanism of action

Peptide presentation for cytotoxic T cell activation Allow drugs or therapies to target antigen expressed in context of HLA-A molecule (e.g., specific TCR interaction with HLA-A2-presented tumor antigen enables cell killing)

03

Biological functions

Immune responseAntigen presentation to cytotoxic T lymphocytesDetection of infected or cancerous cells (cell surveillance)Self/non-self discriminationTriggering apoptosis in abnormal cells
04

Disease associations

Cancer (especially as a target for immunotherapies and as a factor in tumor immune evasion)Infection (especially viral, since HLA-A molecules present viral peptides for immune clearance)Transplantation/rejection (critical for donor-recipient matching)AutoimmunityOther (graft-versus-host disease, stem cell transplantation complications)
05

Safety considerations

Risk of transplant rejectionPotential for off-target immune activation and toxicity in T cell-based therapies (due to cross-reactivity)Immune evasion by cancers or viruses through downregulation of HLA molecules
06

Interacting drugs

Peptide-based vaccines targeting antigens presented by HLA-A2 or HLA-A3

2 more in the full profile.

07

Biomarkers

HLA-A2 (positive patients are often selected for certain cancer vaccines or T-cell therapies)HLA-A3 (less common, but used similarly in some infectious disease and immunotherapy studies)Expression level is used in research as a biomarker for prognosis and therapy selection in cancers and infections

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